» Articles » PMID: 35492705

Social Communication of Maternal Immune Activation-Affected Offspring Is Improved by Si-Based Hydrogen-Producing Agent

Overview
Specialty Psychiatry
Date 2022 May 2
PMID 35492705
Authors
Affiliations
Soon will be listed here.
Abstract

Maternal immune activation (MIA) is triggered by infection or autoimmune predisposition during pregnancy, and cytokines produced by MIA are transmitted through the placenta to the fetal brain, implicating at the onset risks and vulnerability for developmental and psychiatric disorders, such as autism spectrum disorder (ASD) and schizophrenia. To address these kinds of problem in child health, we have developed a silicon (Si)-based hydrogen-producing antioxidant (Si-based agent) that continuously and effectively produces hydrogen in the body. Medical hydrogen is known to have antioxidative, anti-inflammatory, and antiapoptotic effects, therefore we applied our Si-based agent as a potential therapeutic agent to MIA. Using a MIA mouse model, we found that the Si-based agent improved the social communication of MIA offspring mice. We also found that the Si-based agent suppressed the expressions of inflammation-associated genes and in the mouse brain. These results demonstrate that the Si-based agent is an effective prophylactic agent against MIA during pregnancy, suggesting that our Si-based agent may be a preventative or therapeutic agent for ASD and other disease risks in child health suppressing MIA damage.

Citing Articles

Possible roles of deep cortical neurons and oligodendrocytes in the neural basis of human sociality.

Usui N Anat Sci Int. 2023; 99(1):34-47.

PMID: 38010534 PMC: 10771383. DOI: 10.1007/s12565-023-00747-1.


Beyond TORCH: A narrative review of the impact of antenatal and perinatal infections on the risk of disability.

Devaraju M, Li A, Ha S, Li M, Shivakumar M, Li H Neurosci Biobehav Rev. 2023; 153:105390.

PMID: 37708918 PMC: 10617835. DOI: 10.1016/j.neubiorev.2023.105390.


Diverse Possibilities of Si-Based Agent, a Unique New Antioxidant.

Koyama Y, Kobayashi Y, Kobayashi H, Shimada S Antioxidants (Basel). 2023; 12(5).

PMID: 37237927 PMC: 10215636. DOI: 10.3390/antiox12051061.


Neuroinflammation and Oxidative Stress in the Pathogenesis of Autism Spectrum Disorder.

Usui N, Kobayashi H, Shimada S Int J Mol Sci. 2023; 24(6).

PMID: 36982559 PMC: 10049423. DOI: 10.3390/ijms24065487.


Genomic Strategies for Understanding the Pathophysiology of Autism Spectrum Disorder.

Doi M, Li M, Usui N, Shimada S Front Mol Neurosci. 2022; 15:930941.

PMID: 35813066 PMC: 9263364. DOI: 10.3389/fnmol.2022.930941.

References
1.
Garcia-Flores V, Romero R, Xu Y, Theis K, Arenas-Hernandez M, Miller D . Maternal-fetal immune responses in pregnant women infected with SARS-CoV-2. Nat Commun. 2022; 13(1):320. PMC: 8766450. DOI: 10.1038/s41467-021-27745-z. View

2.
Meyer U . Neurodevelopmental Resilience and Susceptibility to Maternal Immune Activation. Trends Neurosci. 2019; 42(11):793-806. DOI: 10.1016/j.tins.2019.08.001. View

3.
Usui N, Araujo D, Kulkarni A, Co M, Ellegood J, Harper M . Foxp1 regulation of neonatal vocalizations via cortical development. Genes Dev. 2017; 31(20):2039-2055. PMC: 5733496. DOI: 10.1101/gad.305037.117. View

4.
Jones S, Jenkins B . Recent insights into targeting the IL-6 cytokine family in inflammatory diseases and cancer. Nat Rev Immunol. 2018; 18(12):773-789. DOI: 10.1038/s41577-018-0066-7. View

5.
Guma E, Bordignon P, Devenyi G, Gallino D, Anastassiadis C, Cvetkovska V . Early or Late Gestational Exposure to Maternal Immune Activation Alters Neurodevelopmental Trajectories in Mice: An Integrated Neuroimaging, Behavioral, and Transcriptional Study. Biol Psychiatry. 2021; 90(5):328-341. DOI: 10.1016/j.biopsych.2021.03.017. View